Maier Timo, Haraszti Tamás
Max Planck Institute for Intelligent Systems, Department of New Materials and Biosystems, Heisenberg str. 3, D-70569 Stuttgart, Germany; University of Heidelberg, Institute of Physical Chemistry, Department of Biophysical Chemistry, Im Neuenheimer Feld 253, D-69120 Heidelberg, Germany.
PLoS One. 2015 Aug 31;10(8):e0136432. doi: 10.1371/journal.pone.0136432. eCollection 2015.
Filamentous actin is one of the most important cytoskeletal elements. Not only is it responsible for the elastic properties of many cell types, but it also plays a vital role in cellular adhesion and motility. Understanding the bundling kinetics of actin filaments is important in the formation of various cytoskeletal structures, such as filopodia and stress fibers. Utilizing a unique pillar-structured microfluidic device, we investigated the time dependence of bundling kinetics of pillar supported free-standing actin filaments. Microparticles attached to the filaments allowed the measurement of thermal motion, and we found that bundling takes place at lower concentrations than previously found in 3-dimensional actin gels, i.e. actin filaments formed bundles in the presence of 5-12 mM of magnesium chloride in a time-dependent manner. The filaments also displayed long term stability for up to hours after removing the magnesium ions from the buffer, which suggests that there is an extensive hysteresis between cation induced crosslinking and decrosslinking.
丝状肌动蛋白是最重要的细胞骨架成分之一。它不仅负责多种细胞类型的弹性特性,还在细胞黏附和运动中起着至关重要的作用。了解肌动蛋白丝的成束动力学对于各种细胞骨架结构(如丝状伪足和应力纤维)的形成很重要。利用一种独特的柱形微流控装置,我们研究了柱支撑的独立肌动蛋白丝成束动力学的时间依赖性。附着在丝上的微粒使得能够测量热运动,并且我们发现成束发生的浓度比先前在三维肌动蛋白凝胶中发现的浓度更低,即肌动蛋白丝在存在5 - 12 mM氯化镁的情况下以时间依赖性方式形成束。在从缓冲液中去除镁离子后,这些丝还显示出长达数小时的长期稳定性,这表明阳离子诱导的交联和解交联之间存在广泛的滞后现象。